Imaging findings of mucopolysaccharidoses: a pictorial review

INTRODUCTION: Mucopolysaccharidosis (MPS) represent a heterogeneous group of inheritable lysosomal storage diseases in which the accumulation of undegraded glycosaminoglycans (GAGs) leads to progressive damage of affected tissues. The typical symptoms include organomegaly, dysostosis multiplex, ment...

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Bibliografski detalji
Glavni autori: Palmucci, Stefano, Attinà, Giancarlo, Lanza, Maria Letizia, Belfiore, Giuseppe, Cappello, Giuseppina, Foti, Pietro Valerio, Milone, Pietro, Di Bella, Domenico, Barone, Rita, Fiumara, Agata, Sorge, Giovanni, Ettorre, Giovanni Carlo
Format: Artigo
Jezik:Inglês
Izdano: Springer Berlin Heidelberg 2013
Teme:
Pictorial Review
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3731470/
https://ncbi.nlm.nih.gov/pubmed/23645566
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13244-013-0246-8
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